In addition, 25% (2 individuals) ofsubjects had phospho-TDP-43-proteinopathy: one case compatible with FTD/ALS(diagnosis based on neuropathological findings and clinical manifestations from themedical specialist records kept when patient was in hospital) associated with ALBPBraak stage I-II, and another case of ALBP Braak stages V-VI. The gene discussed is TARDBP; the disease is amyotrophic lateral sclerosis.